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A proteo-transcriptomic map of non-alcoholic fatty liver disease signatures

Non-alcoholic fatty liver disease (NAFLD) is a common, progressive liver disease strongly associated with the metabolic syndrome. It is unclear how progression of NAFLD towards cirrhosis translates into systematic changes in circulating proteins. Here, we provide a detailed proteo-transcriptomic map...

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Autores principales: Govaere, Olivier, Hasoon, Megan, Alexander, Leigh, Cockell, Simon, Tiniakos, Dina, Ekstedt, Mattias, Schattenberg, Jörn M., Boursier, Jerome, Bugianesi, Elisabetta, Ratziu, Vlad, Daly, Ann K., Anstee, Quentin M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10132975/
https://www.ncbi.nlm.nih.gov/pubmed/37037945
http://dx.doi.org/10.1038/s42255-023-00775-1
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author Govaere, Olivier
Hasoon, Megan
Alexander, Leigh
Cockell, Simon
Tiniakos, Dina
Ekstedt, Mattias
Schattenberg, Jörn M.
Boursier, Jerome
Bugianesi, Elisabetta
Ratziu, Vlad
Daly, Ann K.
Anstee, Quentin M.
author_facet Govaere, Olivier
Hasoon, Megan
Alexander, Leigh
Cockell, Simon
Tiniakos, Dina
Ekstedt, Mattias
Schattenberg, Jörn M.
Boursier, Jerome
Bugianesi, Elisabetta
Ratziu, Vlad
Daly, Ann K.
Anstee, Quentin M.
author_sort Govaere, Olivier
collection PubMed
description Non-alcoholic fatty liver disease (NAFLD) is a common, progressive liver disease strongly associated with the metabolic syndrome. It is unclear how progression of NAFLD towards cirrhosis translates into systematic changes in circulating proteins. Here, we provide a detailed proteo-transcriptomic map of steatohepatitis and fibrosis during progressive NAFLD. In this multicentre proteomic study, we characterize 4,730 circulating proteins in 306 patients with histologically characterized NAFLD and integrate this with transcriptomic analysis in paired liver tissue. We identify circulating proteomic signatures for active steatohepatitis and advanced fibrosis, and correlate these with hepatic transcriptomics to develop a proteo-transcriptomic signature of 31 markers. Deconvolution of this signature by single-cell RNA sequencing reveals the hepatic cell types likely to contribute to proteomic changes with disease progression. As an exemplar of use as a non-invasive diagnostic, logistic regression establishes a composite model comprising four proteins (ADAMTSL2, AKR1B10, CFHR4 and TREM2), body mass index and type 2 diabetes mellitus status, to identify at-risk steatohepatitis.
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spelling pubmed-101329752023-04-28 A proteo-transcriptomic map of non-alcoholic fatty liver disease signatures Govaere, Olivier Hasoon, Megan Alexander, Leigh Cockell, Simon Tiniakos, Dina Ekstedt, Mattias Schattenberg, Jörn M. Boursier, Jerome Bugianesi, Elisabetta Ratziu, Vlad Daly, Ann K. Anstee, Quentin M. Nat Metab Letter Non-alcoholic fatty liver disease (NAFLD) is a common, progressive liver disease strongly associated with the metabolic syndrome. It is unclear how progression of NAFLD towards cirrhosis translates into systematic changes in circulating proteins. Here, we provide a detailed proteo-transcriptomic map of steatohepatitis and fibrosis during progressive NAFLD. In this multicentre proteomic study, we characterize 4,730 circulating proteins in 306 patients with histologically characterized NAFLD and integrate this with transcriptomic analysis in paired liver tissue. We identify circulating proteomic signatures for active steatohepatitis and advanced fibrosis, and correlate these with hepatic transcriptomics to develop a proteo-transcriptomic signature of 31 markers. Deconvolution of this signature by single-cell RNA sequencing reveals the hepatic cell types likely to contribute to proteomic changes with disease progression. As an exemplar of use as a non-invasive diagnostic, logistic regression establishes a composite model comprising four proteins (ADAMTSL2, AKR1B10, CFHR4 and TREM2), body mass index and type 2 diabetes mellitus status, to identify at-risk steatohepatitis. Nature Publishing Group UK 2023-04-10 2023 /pmc/articles/PMC10132975/ /pubmed/37037945 http://dx.doi.org/10.1038/s42255-023-00775-1 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Letter
Govaere, Olivier
Hasoon, Megan
Alexander, Leigh
Cockell, Simon
Tiniakos, Dina
Ekstedt, Mattias
Schattenberg, Jörn M.
Boursier, Jerome
Bugianesi, Elisabetta
Ratziu, Vlad
Daly, Ann K.
Anstee, Quentin M.
A proteo-transcriptomic map of non-alcoholic fatty liver disease signatures
title A proteo-transcriptomic map of non-alcoholic fatty liver disease signatures
title_full A proteo-transcriptomic map of non-alcoholic fatty liver disease signatures
title_fullStr A proteo-transcriptomic map of non-alcoholic fatty liver disease signatures
title_full_unstemmed A proteo-transcriptomic map of non-alcoholic fatty liver disease signatures
title_short A proteo-transcriptomic map of non-alcoholic fatty liver disease signatures
title_sort proteo-transcriptomic map of non-alcoholic fatty liver disease signatures
topic Letter
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10132975/
https://www.ncbi.nlm.nih.gov/pubmed/37037945
http://dx.doi.org/10.1038/s42255-023-00775-1
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